Canonical Allele Identifier: CA2973109354

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209444_201209445insGGAAGTGGGTGCCTGCTC , CM000664.2:g.201209444_201209445insGGAAGTGGGTGCCTGCTC	GRCh38
NC_000002.11:g.202074167_202074168insGGAAGTGGGTGCCTGCTC , CM000664.1:g.202074167_202074168insGGAAGTGGGTGCCTGCTC	GRCh37
NC_000002.10:g.201782412_201782413insGGAAGTGGGTGCCTGCTC	NCBI36
NG_007265.1:g.31313_31314insGGAAGTGGGTGCCTGCTC , LRG_33:g.31313_31314insGGAAGTGGGTGCCTGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1096_1097insGGAAGTGGGTGCCTGCTC	ENSP00000314599.7:p.Glu366delinsGlyLysTrpValProAlaGln
ENST00000346817.10:c.1168_1169insGGAAGTGGGTGCCTGCTC	ENSP00000237865.7:p.Glu390delinsGlyLysTrpValProAlaGln
ENST00000438843.6:c.*754_*755insGGAAGTGGGTGCCTGCTC	ENSP00000401914.1:n.*754_*755insGGAAGTGGGTGCCTGCTC
ENST00000492363.6:c.*383_*384insGGAAGTGGGTGCCTGCTC	ENSP00000512459.1:n.*383_*384insGGAAGTGGGTGCCTGCTC
ENST00000696199.1:c.721+5678_721+5679insGGAAGTGGGTGCCTGCTC	ENSP00000512481.1:n.721+5678_721+5679insGGAAGTGGGTGCCTGCTC
ENST00000286186.11:c.1297_1298insGGAAGTGGGTGCCTGCTC MANE Select	ENSP00000286186.6:p.Glu433delinsGlyLysTrpValProAlaGln
ENST00000272879.9:c.1297_1298insGGAAGTGGGTGCCTGCTC	ENSP00000272879.5:p.Glu433delinsGlyLysTrpValProAlaGln
ENST00000286186.10:c.1297_1298insGGAAGTGGGTGCCTGCTC	ENSP00000286186.6:p.Glu433delinsGlyLysTrpValProAlaGln
ENST00000313728.11:c.1096_1097insGGAAGTGGGTGCCTGCTC	ENSP00000314599.7:p.Glu366delinsGlyLysTrpValProAlaGln
ENST00000346817.9:c.1168_1169insGGAAGTGGGTGCCTGCTC	ENSP00000237865.7:p.Glu390delinsGlyLysTrpValProAlaGln
ENST00000360132.7:c.*383_*384insGGAAGTGGGTGCCTGCTC	ENSP00000353250.3:n.*383_*384insGGAAGTGGGTGCCTGCTC
ENST00000448480.1:c.1168_1169insGGAAGTGGGTGCCTGCTC	ENSP00000396835.1:p.Glu390delinsGlyLysTrpValProAlaGln
ENST00000492363.5:n.1205_1206insGGAAGTGGGTGCCTGCTC
NM_001206524.1:c.1096_1097insGGAAGTGGGTGCCTGCTC	NP_001193453.1:p.Glu366delinsGlyLysTrpValProAlaGln
NM_001206542.1:c.1168_1169insGGAAGTGGGTGCCTGCTC	NP_001193471.1:p.Glu390delinsGlyLysTrpValProAlaGln
NM_001230.4:c.1168_1169insGGAAGTGGGTGCCTGCTC	NP_001221.2:p.Glu390delinsGlyLysTrpValProAlaGln
NM_032974.4:c.1297_1298insGGAAGTGGGTGCCTGCTC	NP_116756.2:p.Glu433delinsGlyLysTrpValProAlaGln
NM_032976.3:c.*383_*384insGGAAGTGGGTGCCTGCTC	NP_116758.1:n.*383_*384insGGAAGTGGGTGCCTGCTC
NM_032977.3:c.1297_1298insGGAAGTGGGTGCCTGCTC , LRG_33t1:c.1297_1298insGGAAGTGGGTGCCTGCTC	NP_116759.2:p.Glu433delinsGlyLysTrpValProAlaGln
XM_005246907.2:c.1294_1295insGGAAGTGGGTGCCTGCTC	XP_005246964.1:p.Glu432delinsGlyLysTrpValProAlaGln
XM_006712796.2:c.547_548insGGAAGTGGGTGCCTGCTC	XP_006712859.1:p.Glu183delinsGlyLysTrpValProAlaGln
XM_006712796.3:c.547_548insGGAAGTGGGTGCCTGCTC	XP_006712859.1:p.Glu183delinsGlyLysTrpValProAlaGln
NM_001206524.2:c.1096_1097insGGAAGTGGGTGCCTGCTC	NP_001193453.1:p.Glu366delinsGlyLysTrpValProAlaGln
NM_001206542.2:c.1168_1169insGGAAGTGGGTGCCTGCTC	NP_001193471.1:p.Glu390delinsGlyLysTrpValProAlaGln
NM_001230.5:c.1168_1169insGGAAGTGGGTGCCTGCTC	NP_001221.2:p.Glu390delinsGlyLysTrpValProAlaGln
NM_032974.5:c.1297_1298insGGAAGTGGGTGCCTGCTC	NP_116756.2:p.Glu433delinsGlyLysTrpValProAlaGln
NM_032977.4:c.1297_1298insGGAAGTGGGTGCCTGCTC MANE Select	NP_116759.2:p.Glu433delinsGlyLysTrpValProAlaGln
NM_032976.4:c.*383_*384insGGAAGTGGGTGCCTGCTC	NP_116758.1:n.*383_*384insGGAAGTGGGTGCCTGCTC